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The predictive value of human papillomavirus testing for the outcome of patients conservatively treated for stage IA squamous cell cervical carcinoma.
Costa, Silvano; Sideri, Mario; Negri, Giovanni; Venturoli, Simona; Santini, Donatella; Casadio, Chiara; Sandri, Maria T; Bucchi, Lauro.
Afiliação
  • Costa S; Department of Obstetrics and Gynaecology, St. Orsola-Malpighi University Hospital, Bologna, Italy.
  • Sideri M; Preventive Gynaecology Unit, European Institute of Oncology, Milano, Italy.
  • Negri G; Department of Pathology, Central Hospital of Bolzano, Bolzano, Italy.
  • Venturoli S; Department of Haematology, Oncology and Laboratory Medicine, Section of Microbiology, St. Orsola-Malpighi University Hospital, Bologna, Italy.
  • Santini D; Department of Pathology, St. Orsola-Malpighi University Hospital, Bologna, Italy.
  • Casadio C; Cytology Unit, Department of Pathology, European Institute of Oncology, Milano, Italy.
  • Sandri MT; Division of Laboratory Medicine, European Institute of Oncology, Milano, Italy.
  • Bucchi L; Romagna Cancer Registry, Romagna Cancer Institute (IRST), Meldola, Forlì, Italy. Electronic address: lauro.bucchi@irst.emr.it.
J Clin Virol ; 70: 53-57, 2015 Sep.
Article em En | MEDLINE | ID: mdl-26305820
ABSTRACT

BACKGROUND:

Although it is hypothesised that human papillomavirus (HPV) testing may have a role in surveillance of patients conservatively treated for stage IA squamous cell cervical carcinoma, research on this topic has been minimal.

OBJECTIVES:

To determine (1) the changes in HPV test result from treatment onward; (2) the time to viral clearance; and (3) the negative predictive value (NPV) and positive predictive value (PPV) of HPV test result for the detection of CIN2 or worse (CIN2+) during follow-up. STUDY

DESIGN:

In a multicentre retrospective follow-up study of a consecutive series (1997-2009) of 91 patients, longitudinal outcome measures were estimated as cumulative probabilities using the Kaplan-Meier method.

RESULTS:

For patients testing HPV-positive at the first follow-up visit (n=44), the probability of change to negative rose from 0 to 0.78 between 7 and 21 months after treatment. For HPV-negative patients (n=47), the probability of change to positive rose to 0.13 between 9 and 26 months. After a median follow-up of 50 months (range, 2-80), the NPV for CIN2+ was 1.00. The PPV was 0.60 (95% confidence interval, 0.43-0.77) after 26 months. The median time to detection was 5 months.

CONCLUSIONS:

If adequately confirmed, these findings would indicate that HPV testing is capable to identify the patients who have had their lesions fully removed, and would make it possible to focus follow-up efforts on a subset of patients at high risk of residual or progressive disease.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Papillomaviridae / Carcinoma de Células Escamosas / Neoplasias do Colo do Útero / Infecções por Papillomavirus Tipo de estudo: Diagnostic_studies / Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Aged / Female / Humans / Middle aged Idioma: En Revista: J Clin Virol Assunto da revista: VIROLOGIA Ano de publicação: 2015 Tipo de documento: Article País de afiliação: Itália

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Papillomaviridae / Carcinoma de Células Escamosas / Neoplasias do Colo do Útero / Infecções por Papillomavirus Tipo de estudo: Diagnostic_studies / Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Aged / Female / Humans / Middle aged Idioma: En Revista: J Clin Virol Assunto da revista: VIROLOGIA Ano de publicação: 2015 Tipo de documento: Article País de afiliação: Itália